NDC 67046-171

Escitalopram

Escitalopram

Escitalopram is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Contract Pharmacy Services-pa. The primary component is Escitalopram Oxalate.

Product ID67046-171_5a084ea4-cafd-ffed-e053-2991aa0aa0d9
NDC67046-171
Product TypeHuman Prescription Drug
Proprietary NameEscitalopram
Generic NameEscitalopram
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2017-09-25
Marketing CategoryANDA / ANDA
Application NumberANDA076765
Labeler NameContract Pharmacy Services-PA
Substance NameESCITALOPRAM OXALATE
Active Ingredient Strength10 mg/1
Pharm ClassesSerotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 67046-171-07

7 TABLET, FILM COATED in 1 BLISTER PACK (67046-171-07)
Marketing Start Date2017-09-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 67046-171-30 [67046017130]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-20 [67046017120]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-07 [67046017107]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-28 [67046017128]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-14 [67046017114]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-21 [67046017121]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-15 [67046017115]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

NDC 67046-171-60 [67046017160]

Escitalopram TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA076765
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-09-25
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ESCITALOPRAM OXALATE10 mg/1

OpenFDA Data

SPL SET ID:5a084ea4-cafc-ffed-e053-2991aa0aa0d9
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349332
    • UPC Code
  • 0300935851013

    • Pharmacological Class

    • Serotonin Reuptake Inhibitor [EPC]
    • Serotonin Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Escitalopram" or generic name "Escitalopram"

    NDCBrand NameGeneric Name
    0093-5850EscitalopramEscitalopram
    0093-5851EscitalopramEscitalopram
    0093-5852EscitalopramEscitalopram
    0143-9807EscitalopramEscitalopram
    0143-9808EscitalopramEscitalopram
    0143-9809EscitalopramEscitalopram
    0615-7720EscitalopramEscitalopram
    0615-7721EscitalopramEscitalopram
    0615-7722EscitalopramEscitalopram
    0615-7953EscitalopramEscitslopram
    0615-7954EscitalopramEscitslopram
    0615-7955EscitalopramEscitslopram
    0615-8348EscitalopramEscitalopram
    0615-8349EscitalopramEscitalopram
    0615-8350EscitalopramEscitalopram
    0615-8365EscitalopramEscitalopram
    0615-8366EscitalopramEscitalopram
    16729-168EscitalopramEscitalopram
    68001-195EscitalopramEscitalopram
    68001-196EscitalopramEscitalopram
    68001-197EscitalopramEscitalopram
    68071-2051EscitalopramEscitalopram
    68071-3069EscitalopramEscitalopram
    68071-2035EscitalopramEscitalopram
    68071-4332EscitalopramEscitalopram
    68071-4484EscitalopramEscitalopram
    68084-617EscitalopramEscitalopram
    68084-618EscitalopramEscitalopram
    68180-135EscitalopramEscitalopram
    68180-136EscitalopramEscitalopram
    68180-137EscitalopramEscitalopram
    68258-7128EscitalopramEscitalopram
    68382-103escitalopramescitalopram
    68382-104escitalopramescitalopram
    68382-102escitalopramescitalopram
    68788-6837EscitalopramEscitalopram
    68788-6403EscitalopramEscitalopram
    68788-6783EscitalopramEscitalopram
    68788-9302EscitalopramEscitalopram
    68788-9456EscitalopramEscitalopram
    68788-9714EscitalopramEscitalopram
    70518-0692EscitalopramEscitalopram
    70518-1110EscitalopramEscitalopram
    70518-0758EscitalopramEscitalopram
    70518-1103EscitalopramEscitalopram
    70518-1857EscitalopramEscitalopram
    70518-1876EscitalopramEscitalopram
    70518-1785EscitalopramEscitalopram
    70518-1805EscitalopramEscitalopram
    70771-1145escitalopramescitalopram
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